HGVS | Genome Assembly |
---|---|
NC_000011.10:g.118312726A>G , CM000673.2:g.118312726A>G | GRCh38 |
NC_000011.9:g.118183441A>G , CM000673.1:g.118183441A>G | GRCh37 |
NC_000011.8:g.117688651A>G | NCBI36 |
NG_007383.1:g.13147A>G , LRG_38:g.13147A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361763.9:c.212A>G MANE Select | ENSP00000354566.4:p.Asp71Gly | |
ENST00000361763.8:c.212A>G | ENSP00000354566.4:p.Asp71Gly | |
ENST00000526146.5:n.758A>G | ||
ENST00000528435.5:n.765A>G | ||
ENST00000528600.1:c.194A>G | ENSP00000433975.1:p.Asp65Gly | |
ENST00000529713.5:n.318A>G | ||
ENST00000531913.1:n.583A>G | ||
NM_000733.3:c.212A>G , LRG_38t1:c.212A>G | NP_000724.1:p.Asp71Gly | |
NM_000733.4:c.212A>G MANE Select | NP_000724.1:p.Asp71Gly |